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Summary Literature (0)
DOID:0111153 - congenital mirror movement disorder

Disease Ontology Definition:A movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs.

Synonyms: familial congenital controlateral synkinesia, familial congenital mirror movements, hereditary congenital controlateral synkinesia, hereditary congenital mirror movements, isolated congenital controlateral synkinesia, isolated congenital mirror movements

In Mondo Disease Ontology:
MONDO:0016558 - familial congenital mirror movements

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : dcc, dnal4, ntn1, rad51

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): movement disease (is_a), physical disorder (is_a)